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B A Gordon

Showing results (1-10 of 46) with videos related to

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Clinical Biochemistry|April 1, 1971
Leukocyte hydrolases in the Sanfilippo syndromeB A Gordon, V Feleki
Clinical Biochemistry|September 1, 1970
Acid hydrolases in the serum and liver in mucopolysaccharidoses types I and 3B A Gordon, V Feleki
Connective Tissue Research|January 1, 1986
Ultrastructural and biochemical aspects of the Sanfilippo syndrome,--type III genetic mucopolysaccharidosisM D Haust, B A Gordon
Clinical Biochemistry|April 29, 1998
A simple spectrophotometric enzyme assay with absolute specificity for arylsulfatase AJ W Rip, B A Gordon
Canadian Medical Association Journal|August 7, 1976
Methylmalonic acidemia controlled with oral administration of vitamin B12B A Gordon, R A Carson
Pediatric Research|December 1, 1980
Ultrastructural changes in the mitochondria in disorders in ornithine metabolismM D Haust, B A Gordon
Birth Defects Original Article Series|January 1, 1987
Possible pathogenetic mechanism in hyperornithinemia, hyperammonemia, and homocitrullinuria syndromeM D Haust, B A Gordon
Clinical Biochemistry|June 1, 1991
Defective expression of alpha-L-fucosidase by lymphoid cells of a fucosidosis patientR A DiCioccio, B A Gordon
Clinical Biochemistry|September 1, 1970
The mucopolysaccharidoses types I, II, and 3: urinary findings in 23 casesB A Gordon, M D Haust
Clinical Biochemistry|October 1, 1971
Hepatic acid mucopolysaccharides in the mucopolysaccharidoses type I, II and 3B A Gordon, M D Haust
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
Clinical Biochemistry|April 1, 1971
Leukocyte hydrolases in the Sanfilippo syndromeB A Gordon, V Feleki
Clinical Biochemistry|September 1, 1970
Acid hydrolases in the serum and liver in mucopolysaccharidoses types I and 3B A Gordon, V Feleki
Connective Tissue Research|January 1, 1986
Ultrastructural and biochemical aspects of the Sanfilippo syndrome,--type III genetic mucopolysaccharidosisM D Haust, B A Gordon
Clinical Biochemistry|April 29, 1998
A simple spectrophotometric enzyme assay with absolute specificity for arylsulfatase AJ W Rip, B A Gordon
Canadian Medical Association Journal|August 7, 1976
Methylmalonic acidemia controlled with oral administration of vitamin B12B A Gordon, R A Carson
Pediatric Research|December 1, 1980
Ultrastructural changes in the mitochondria in disorders in ornithine metabolismM D Haust, B A Gordon
Birth Defects Original Article Series|January 1, 1987
Possible pathogenetic mechanism in hyperornithinemia, hyperammonemia, and homocitrullinuria syndromeM D Haust, B A Gordon
Clinical Biochemistry|June 1, 1991
Defective expression of alpha-L-fucosidase by lymphoid cells of a fucosidosis patientR A DiCioccio, B A Gordon
Clinical Biochemistry|September 1, 1970
The mucopolysaccharidoses types I, II, and 3: urinary findings in 23 casesB A Gordon, M D Haust
Clinical Biochemistry|October 1, 1971
Hepatic acid mucopolysaccharides in the mucopolysaccharidoses type I, II and 3B A Gordon, M D Haust
Pageof 5